- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as a Senior Director , Pharmacovigilance (PV) Operations in Cambridge, MA, where ... you will provide leadership and oversight to Global and Regional PV Operational Teams to ensure adverse...marketing services. As part of the Patient Safety & Pharmacovigilance (PSPV) team you will report to the Executive… more
- Takeda Pharmaceuticals (Boston, MA)
- …+ Technically fully competent to perform all usual Principal Pharmacovigilance Scientist/ Senior Pharmacovigilance Scientist workload, including ... life-changing therapies to patients worldwide. Join Takeda as a Senior Principal Pharmacovigilance Scientist in the Neuroscience... Medical Safety team, you will report to the Senior Medical Director , GI and work with… more
- Boehringer Ingelheim (Ridgefield, CT)
- …you with the opportunity for significant professional development. The ( Senior Associate) Director is a key member of global , cross functional product teams ... **Description** The ( Senior Associate) Director will join our...of team members, review of team output + Represent Global Pharmacovigilance in internal and external committees… more
- Takeda Pharmaceuticals (Boston, MA)
- …Management and Education function, you will report to the Senior Director , Signal Management and represent the pharmacovigilance department as subject matter ... to bring life-changing therapies to patients worldwide. Join Takeda as a Associate Director , Global Patient Safety Signal Management and Innovation in Cambridge,… more
- Gilead Sciences, Inc. (Foster City, CA)
- …in Patient Safety cross-functional teams. + Communicates to highest levels of senior management key pharmacovigilance findings. + Oversees or performs medical ... preferred. + A minimum of 6 years' experience in pharmacovigilance with substantial knowledge of drug safety including medical...review of ICSRs. + Extensive knowledge of US and global ICSR medical review regulations and IND Safety Reporting.… more
- Teva Pharmaceuticals (Parsippany, NJ)
- Senior Director Clinical Development - Respiratory Date: Aug 31, 2024 Location: Parsippany, United States, New Jersey, 07054 Company: Teva Pharmaceuticals Job ... be based in Parsippany, NJ or West Chester, PA Senior Director , Clinical Development is responsible for...Resolves safety or relevant clinical issues in consultation with Global Drug Safety and Pharmacovigilance , SVP Late… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …Affairs Oncology team, you will report to the Head of Medical Capabilities, Global Medical Affairs Oncology and work with Pharmacovigilance /QA and Legal teams. ... **How you will contribute:** + The Director , Global Medical Information & Review will...is relationship management with key stakeholder groups such as pharmacovigilance , therapeutic leads, quality assurance and other functions to… more
- Boehringer Ingelheim (Ridgefield, CT)
- …in the global Inflammation Therapeutic Area of Patient Safety and Pharmacovigilance at BI, whose priority is the wellbeing of our patients worldwide. This ... and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering… more
- Bristol Myers Squibb (Princeton, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Senior Director , Risk Based Quality Management leader will work closely ... an effective quality and compliance govervance model across nonclinical, clinical and pharmacovigilance in line with Global Quality. + Drive the effective… more
- Takeda Pharmaceuticals (Boston, MA)
- …company that will inspire you and empower you to shine? Join us as a Senior Medical Director , GI TAU- Hematology in our Cambridge, MA office. At Takeda, ... world. Here, you will be a vital contributor to our inspiring, bold mission. The Senior Medical Director , GI TAU- Hematology leads and drives strategy for the… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …researching on real-world evidence, and creating hope for all facing illness. The Senior Director , Regulatory Affairs - Clinical (Neuroderm), may be called upon ... practical, workable plans to facilitate timely drug development and registration. The Senior Director , Regulatory Affairs - Clinical also works directly with… more
- Bristol Myers Squibb (Madison, NJ)
- …in their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Senior Medical Director , US Lymphoma/CLL will report to the ... will lead the US medical Lymphoma team supporting the MM/Lymphoma Disease Lead. The Senior Medical Director will provide key contribution for the overall medical… more
- BeiGene (Emeryville, CA)
- **General Description:** The Senior Medical Director , Hematology will support BeiGene Clinical and Medical Hematology assets by successful execution of clinical ... and collaboration partners. The candidate will report to the Vice President, Global Clinical Development. As a leader in the organization, the incumbent will… more
- BeiGene (San Mateo, CA)
- The Senior Director , Clinical Development, Solid Tumors will support BeiGene Clinical and Medical assets by successful execution of clinical development programs ... establishment and growth of Clinical Research functions to assure best-in-class global capabilities and execution. Specifically, the incumbent will work closely with… more
- BeiGene (San Mateo, CA)
- **General** **Description:** The Senior Director , Clinical Science will support BeiGene Clinical and Medical assets by successful execution of clinical ... establishment and growth of Clinical Research functions to assure best-in-class global capabilities and execution. Specifically, the incumbent will work closely with… more
- AbbVie (North Chicago, IL)
- …understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. Serves ... key regulatory discussions. + Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality… more
- AbbVie (Irvine, CA)
- …understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. Serves ... key regulatory discussions. + Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …capabilities in translational studies and with external scientific experts. Reporting into the Senior Director of the Translational Medicine (TM) group, the ... pharmaceutical company that has tirelessly pursued medical breakthroughs with global reach. MTPC has discovered and produced several first-in-class medicines… more
- Takeda Pharmaceuticals (Boston, MA)
- …Safety & Pharmacovigilance (PSPV) team, you will report to the Director and Head, PV Document Management (PVDM). **How you will** **contribute:** + Provides ... order to bring life-changing therapies to patients worldwide. Join Takeda as a Senior Manager, Aggregate Safety Reporting in Cambridge, MA, where you will be… more
- AbbVie (North Chicago, IL)
- …or product indications under the direction of the Therapeutic Area (TA) Lead and Global TA. Ensuring safety of one or more products through the product lifecycle (eg ... signal detection, validation and assessment). Interpreting regulations related to pharmacovigilance supporting all patient safety activities. Responsibilities: + Understanding… more